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Update on Lymphoma

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Old Dec 16, 2010 | 12:15 PM
  #41  
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Deb,

So happy to hear! My wife will be super happy to hear as well. I'm sure you'll hear from her via FB - just sent her a text.

'Tis the season for miracles...

If you need anything please let us know.

Charlie

Last edited by cjlaw73; Dec 16, 2010 at 12:18 PM.
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Old Dec 16, 2010 | 12:29 PM
  #42  
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Originally Posted by gnmontagnino
Deb i am into my 13th treatment and have 26 more to go. I have started to feel the side affects of radiation it is not pleasant when you have any of these treatments. I am up at 5am out the door at 6:30 off to the hospital back home and off to work. My radiation is like a second job but as you know it is a must if we want to beat this dreaded disease. I sometimes sit alone and get very depressed but then i will get an email from Carmen or Bob that will make me smile and they always have positive wishes when i talk to them. I am sorry you have no family in the NY area if you ever need a ear to listen to you i will gladly send you my cell phone number. I have found it is very comforting to talk to someone who has or is going through this illness. I will hopefully be down at the Docs after the holidays. I am having my calipers powder coated and Carmen will be taking care of that for me.I will let you know when i pick up the car maybe i will see you then. Stay strong
gnmontagnino, hang in there, I did the radiation/chemo concurrently route for my lung cancer and have to say as easy as the radiation treatments were (you just lay there) once the effects kick in they are the hardest to deal with. My esphogus was so enflamed it hurt to eat jello, it was too solid, ice cream and pudding were much easier but still tough to get down. They even gave me my pain medication oxycodone in liquid form (what I would give for a bottle of that now. j/k) I also got periocariditus sp? from it. Hopefully you will fair a lot better than me, they did say that I got every side effect and that I was not the norm. That said, it was all worth it and is all a distant memory now. I know, you were probably saying to yourself for me to get to the point. Well that is it, it will soon be a distant memory and you will be glad it is over and are cancer free. They put me on anti depressants despite me thinking I did not need or want them but I have to say they were god sent. IF you are not already on them ask your doctor for a script, they REALLY help with your mental outlook while you are going on treatments. I remember sitting in the HUP Radiation ward every day and it was very depressing seeing the other patients, especially when they would bring the babies in from CHOP for the treatments. It would bring tears to my eyes. Well, I am not going to tell you any stories because I do not want to depress you any more. I will tell you they gave me a 5% 5 year survival rate since I was stage 3b lung cancer and I have been cancer free for 12 years now. Like I told Deb, somebody has to be in that percentage of survivors and it might as well be us. They are making great strides in the cancer treatment arena and it is no longer a death sentence.

Deb, I am jealous, I would so love to be going to Florida to escape this cold weather. Hopefully some day. You can get some REALLY great deals down there right now on real estate since the market down there is so bad, much worst than up here. You should make out good in that department. Have a great time and enjoy the weather. I hope your mother feels better.

Last edited by agentf1; Dec 16, 2010 at 12:32 PM.
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Old Dec 16, 2010 | 03:09 PM
  #43  
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Originally Posted by agentf1
gnmontagnino, hang in there, I did the radiation/chemo concurrently route for my lung cancer and have to say as easy as the radiation treatments were (you just lay there) once the effects kick in they are the hardest to deal with. My esphogus was so enflamed it hurt to eat jello, it was too solid, ice cream and pudding were much easier but still tough to get down. They even gave me my pain medication oxycodone in liquid form (what I would give for a bottle of that now. j/k) I also got periocariditus sp? from it. Hopefully you will fair a lot better than me, they did say that I got every side effect and that I was not the norm. That said, it was all worth it and is all a distant memory now. I know, you were probably saying to yourself for me to get to the point. Well that is it, it will soon be a distant memory and you will be glad it is over and are cancer free. They put me on anti depressants despite me thinking I did not need or want them but I have to say they were god sent. IF you are not already on them ask your doctor for a script, they REALLY help with your mental outlook while you are going on treatments. I remember sitting in the HUP Radiation ward every day and it was very depressing seeing the other patients, especially when they would bring the babies in from CHOP for the treatments. It would bring tears to my eyes. Well, I am not going to tell you any stories because I do not want to depress you any more. I will tell you they gave me a 5% 5 year survival rate since I was stage 3b lung cancer and I have been cancer free for 12 years now. Like I told Deb, somebody has to be in that percentage of survivors and it might as well be us. They are making great strides in the cancer treatment arena and it is no longer a death sentence.

Deb, I am jealous, I would so love to be going to Florida to escape this cold weather. Hopefully some day. You can get some REALLY great deals down there right now on real estate since the market down there is so bad, much worst than up here. You should make out good in that department. Have a great time and enjoy the weather. I hope your mother feels better.
Thanks for your understanding of what we are going through anyway the side affects have started for me the worse on is i now have to plan my meals around bathroom runs. The side affect that is really hard to deal with when you have prostate cancer radiation treatment is the affect on your bowels. Anyway i do not want to get to graphic but i think you know what i am saying. Like i told Deb and you will agree the best thing to have is as much support and positive karma around you to keep your spirits up!!!!!!!!!!!!!!!!!!!!!! Thanks again hey Deb i am still waiting for your call i guess it is a good thing i have not heard from youThat tells me you are in a good frame of mind stay strong!!!!!! We WILL kick this cancers ***
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Old Dec 16, 2010 | 05:07 PM
  #44  
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Hope for the best for you! I was dianosed with Chronic Lymphomic Leukemia in April of this year. I know how you feel..the worry, tears, fears, and Hope. If ya need a voice or a ear feel free to PM me or email me at ed77katr@verizon.net anytime. I have all the faith in the world for a cure,and plan on making it to a old folks home someday in the far future. I am sure to Perhaps run into you there. We can talk old days about Corvettes there...LOL I plan on dying of senility or alcoholism at a advanced age Good Luck Ed
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Old Dec 16, 2010 | 07:54 PM
  #45  
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So good to hear Deb....it is a time of year for wonderous news I wish you and your son a blessed Christmas and know you have prayer warriors down here!
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Old Dec 17, 2010 | 10:47 PM
  #46  
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Just seen your update today Deb I don't make it to the Forum as much as I used to. Glad to hear things are looking better I can't begin to imagine what you are going through.....Keep fighting!! Wishing you and your son a Happy Holiday
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Old Dec 18, 2010 | 12:04 AM
  #47  
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Stay strong and positive. You have a lot of support and prayers here.

Have a Merry Christmas and hope to see you soon.
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Old Dec 18, 2010 | 09:38 AM
  #48  
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I'm happy to hear that Deb! Stay strong and i'm sure you'll beat it
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Old Dec 23, 2010 | 10:01 PM
  #49  
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Deb, I haven't been logging on to CF much lately but you have been in my thoughts. I am soooo happy that your scan came out clean!! I will keep you in my prayers in the meantime have a great Christmas and if you need anything just holler.
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Old Dec 25, 2010 | 11:37 AM
  #50  
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Merry Christmas Deb. Hope you and Little Alex enjoy every minute of it.
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Old Dec 26, 2010 | 10:56 AM
  #51  
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Originally Posted by cor08vette
Please PM me as the time gets near. I look forward to seeing you.

I will keep you and your Mom in my prayers
Thank you Jesse!! My mom is doing much better and was able to be home enjoying Christmas. I will call you a week or two before we come down so that we can plan a visit!

Originally Posted by CTYANK2
Great to hear that you are winning the battle!
Its a fight every day, but I sure am trying my hardest

Originally Posted by cjlaw73
Deb,

So happy to hear! My wife will be super happy to hear as well. I'm sure you'll hear from her via FB - just sent her a text.

'Tis the season for miracles...

If you need anything please let us know.

Charlie
Charlie, thanks to you and Leah! I responded to Leah on FB - she is just the nicest person!!!!

Originally Posted by agentf1
gnmontagnino, hang in there, I did the radiation/chemo concurrently route for my lung cancer and have to say as easy as the radiation treatments were (you just lay there) once the effects kick in they are the hardest to deal with. My esphogus was so enflamed it hurt to eat jello, it was too solid, ice cream and pudding were much easier but still tough to get down. They even gave me my pain medication oxycodone in liquid form (what I would give for a bottle of that now. j/k) I also got periocariditus sp? from it. Hopefully you will fair a lot better than me, they did say that I got every side effect and that I was not the norm. That said, it was all worth it and is all a distant memory now. I know, you were probably saying to yourself for me to get to the point. Well that is it, it will soon be a distant memory and you will be glad it is over and are cancer free. They put me on anti depressants despite me thinking I did not need or want them but I have to say they were god sent. IF you are not already on them ask your doctor for a script, they REALLY help with your mental outlook while you are going on treatments. I remember sitting in the HUP Radiation ward every day and it was very depressing seeing the other patients, especially when they would bring the babies in from CHOP for the treatments. It would bring tears to my eyes. Well, I am not going to tell you any stories because I do not want to depress you any more. I will tell you they gave me a 5% 5 year survival rate since I was stage 3b lung cancer and I have been cancer free for 12 years now. Like I told Deb, somebody has to be in that percentage of survivors and it might as well be us. They are making great strides in the cancer treatment arena and it is no longer a death sentence.

Deb, I am jealous, I would so love to be going to Florida to escape this cold weather. Hopefully some day. You can get some REALLY great deals down there right now on real estate since the market down there is so bad, much worst than up here. You should make out good in that department. Have a great time and enjoy the weather. I hope your mother feels better.
I think you guys are BOTH amazing!

Originally Posted by ED77KATR
Hope for the best for you! I was dianosed with Chronic Lymphomic Leukemia in April of this year. I know how you feel..the worry, tears, fears, and Hope. If ya need a voice or a ear feel free to PM me or email me at ed77katr@verizon.net anytime. I have all the faith in the world for a cure,and plan on making it to a old folks home someday in the far future. I am sure to Perhaps run into you there. We can talk old days about Corvettes there...LOL I plan on dying of senility or alcoholism at a advanced age Good Luck Ed
I will take that challenge in the old folks home! I've had practice using those rolling valets at the hotels

Originally Posted by qcdoc1
So good to hear Deb....it is a time of year for wonderous news I wish you and your son a blessed Christmas and know you have prayer warriors down here!
Thank you Martin - Merry Christmas to you as well!

Originally Posted by BT-01-vette
Just seen your update today Deb I don't make it to the Forum as much as I used to. Glad to hear things are looking better I can't begin to imagine what you are going through.....Keep fighting!! Wishing you and your son a Happy Holiday
A very Happy New Year to you too Barry, I appreciate the great wishes!

Originally Posted by Marc V.
Stay strong and positive. You have a lot of support and prayers here.

Have a Merry Christmas and hope to see you soon.
Thanks Marc and Merry Christmas

Originally Posted by EPMM 03 C5
I'm happy to hear that Deb! Stay strong and i'm sure you'll beat it
Looking forward to seeing you and Alicia soon.....hope she is feeling great!!!

Originally Posted by stormrider
Deb, I haven't been logging on to CF much lately but you have been in my thoughts. I am soooo happy that your scan came out clean!! I will keep you in my prayers in the meantime have a great Christmas and if you need anything just holler.
Thank you Mark!!! I was just looking at the photos from when Barry and I met you in Carlisle.......great time!!!

Originally Posted by Ralphyboy
Merry Christmas Deb. Hope you and Little Alex enjoy every minute of it.
Thanks Ralph! We sure did......Santa sent one of his special elves to help us out.........did you know Santa had an elf named Clyde????

Merry Christmas and Happy New Year everyone - thank you all so much for remembering me. Thank you to Danny for the constant words of encouragement......

and mostly........thank you Barry....for everything (Merry Christmas Mr. President )
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Old Dec 26, 2010 | 02:49 PM
  #52  
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Originally Posted by TryNkeepUp
and mostly........thank you Barry....for everything (Merry Christmas Mr. President )
Now there is a scary image
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Old Dec 26, 2010 | 04:59 PM
  #53  
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Originally Posted by stormrider
Now there is a scary image
You have no idea!!!



Back to the doc on 1/27 to discuss stem cell transplant options Trying to keep smiling until then!
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Old Dec 27, 2010 | 05:38 PM
  #54  
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Originally Posted by TryNkeepUp
Thank you Jesse!! My mom is doing much better and was able to be home enjoying Christmas. I will call you a week or two before we come down so that we can plan a visit!
That's great! You both are in my prayers
Originally Posted by TryNkeepUp
Back to the doc on 1/27 to discuss stem cell transplant options Trying to keep smiling until then!
Deb, don't ever miss the opportunity to smile today, over something in the future

Deal with the 27th, on the 27th.

You know that we're here for you now, and throughout the entire process

Stay strong!

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Old Dec 27, 2010 | 06:01 PM
  #55  
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Originally Posted by TryNkeepUp
You have no idea!!!



Back to the doc on 1/27 to discuss stem cell transplant options Trying to keep smiling until then!
Keep hanging in there! Better days are ahead.
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Old Dec 27, 2010 | 10:45 PM
  #56  
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positive thoughts... they work wonders


and hey... put this all behind you in 2011 already would ya!!!

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Old Dec 27, 2010 | 11:23 PM
  #57  
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I'm trying Kym.....I'm really trying!! Thank you!! Hope Gunnar enjoyed his first Christmas
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Old Dec 27, 2010 | 11:41 PM
  #58  
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Great to hear from you Sunday! I'm sure with all the folks here that we should be able to scrounge up a few stem cells here and there (I know we can't help you in this matter, but you KNOW we would if we could). I'm sure the stem cells are more of a catch net for the future, and I hope and pray that you'll have no need for them, but look what you have endured over the last 5 months and defied the percentages by beating this horror of a medical adventure (this is what the Tequila is for!) Hope to see you soon!
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Old Dec 28, 2010 | 11:00 PM
  #59  
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Originally Posted by Ol'55
Great to hear from you Sunday! I'm sure with all the folks here that we should be able to scrounge up a few stem cells here and there (I know we can't help you in this matter, but you KNOW we would if we could). I'm sure the stem cells are more of a catch net for the future, and I hope and pray that you'll have no need for them, but look what you have endured over the last 5 months and defied the percentages by beating this horror of a medical adventure (this is what the Tequila is for!) Hope to see you soon!
Loved our three way conversation with RA!! Was soooo good to hear both your voices again! Keep me posted on weather for this weekend and if it looks crappy, then for next. I'm battling a horrible head cold the last two days so hoping that clears up soon.

I have it on pretty good authority that the stem cell transplant won't be too bad - a fairly quick procedure so I'm not scared......just anxious, like "lets get it over with already" ya know?

Tell RA to send me the weather report and I'll be on standby! Will try to get Barry in on this too if I can.....otherwise we'll just have to do it a second time
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Old Dec 29, 2010 | 09:08 AM
  #60  
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Deb, good luck with the stem cell transplant, i would guess to say the chemotherapy was much harder so you should do fine with it.
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